Gene found for deadliest breast cancer

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Perth researchers discover new cancer-causing gene and protein for highly aggressive hard to treat cancer in 10 per cent of hormone sensitive cancer patients. Eight years work by Harry Perkins Institute of Medical Research and UWA's scientist Associate Professor Pilar Blancafort, has resulted in the discovery of a cancer gene responsible for a particularly aggressive breast cancer that is typically resistant to treatment. This research was published today in Nature Communications.

Journal/conference: Nature Communications

Link to research (DOI): 10.1038/s41467-021-22101-7

Organisation/s: Harry Perkins Institute of Medical Research

Funder: N/A

Media release

From: Harry Perkins Institute of Medical Research

MEDIA RELEASE                                                                                                    30 March 2021

FOR IMMEDIATE PUBLICATION

Gene found for deadliest breast cancer - published in Nature Communications

Perth researchers discover new cancer-causing gene and protein for highly aggressive hard-to-treat cancer in sub-group of hormone sensitive breast cancers.

·      Cancer-causing gene produces large amounts of unique protein - AAMDC

·      AAMDC triggers tumour growth in sub-group of hormone sensitive breast cancers

·      Standard treatments for hormone sensitive breast could promote tumour growth in patients carrying high levels of newly discovered cancer-causing gene

Eight years work by Harry Perkins Institute of Medical Research and The University of Western Australia’s scientist Associate Professor Pilar Blancafort, has resulted in the discovery of a cancer gene responsible for a particularly aggressive breast cancer that is typically resistant to treatment.

This research published in Nature Communications investigated hormone sensitive breast cancers, which make up about three quarters of all breast cancers, and which typically have a high survival rate.

The team discovered a previously uncharacterised sub-group of hormone sensitive cancers that are very aggressive and have a poor prognosis.

“Hormone sensitive breast cancers usually have better outcomes than the hormone negative ones, such as triple negative breast cancer.

“However, a small percentage of patients experience a very aggressive cancer that results in the worst outcomes of all breast cancers, with half of all women dying from the disease”, said lead researcher Associate Professor Pilar Blancafort Cancer Epigenetics Head at Perth’s Harry Perkins Institute of Medical Research.

“When we look at these cancers, we find that they are bigger and tend to spread more commonly to lymph nodes and have a higher death rate. What we needed was a way to identify them.

“We began by taking data from a major genomic study in Stanford USA of thousands of breast cancers and looked at the worst types in that group of previously unidentified cancers.

“By analysing this sub-group, we discovered these aggressive cancers have extra copies of a particular oncogene, (cancer causing gene) and we found this gene is used to make a cancer driving protein (AAMDC) at higher than normal levels.

“This amplification of the gene that makes the AAMDC cancer driving protein is found on a particular chromosome – chromosome 11 – in about 10% of all breast cancers.

“It is also present in other cancers, such as ovarian, prostate and lung cancers.

“Importantly we can now find these cancers by looking for high levels of AAMDC in the tumour cells.

“This protein is not like any other yet discovered, it is unique.

“AAMDC has a structure or shape that is different from any other protein so far discovered in the human body.

“In fact, the shape or folding of the new protein most closely resembles a protein found in bacteria, rather than in human cells. Its unique shape suggests that the protein does a different job in normal human cells than all other proteins found so far.

“This protein promotes growth of the cancer, but it is unusual in that it is not triggered by the hormones in breast tissue, estrogen and progesterone, which are typically the major controllers of cell growth.

“In fact this cancer protein protects them against anti-cancer hormone treatments, preventing the cancers from being cured.

“We discovered that the AAMDC protein can reprogram breast cancer cell metabolism, activating growth pathways in the cell and allowing increasing growth and division and making the cells more adaptable when food and energy supplies are low, when estrogen is removed or, similarly, when cancer cells are placed in the presence of anti-estrogens.

“Usually starving hormone receptive breast cancers of estrogen causes them to shrink, but in this sub-group starving them of estrogen triggers a signal that causes the tumour to grow.

“In other words, AAMDC can protect cancer cells from dying and maintain their growth when the tumour is placed in conditions where nutrients are scarce and when it is starved of estrogen which would kill most hormone sensitive cancers.

“Therefore, we believe the cancer promoting function of AAMDC is to act as a ‘survival kit’, allowing tumours to adapt to these conditions supporting the growth and multiplication of breast cancer cells in conditions of metabolic stress.

“Importantly, by using new drugs which block the pathways AAMDC switches on to allow cancer cell survival, we may be able both to kill these cancer cells directly as well as restore their sensitivity to usual hormone treatments.

“Hopefully this will dramatically improve the poor outcomes these patients currently suffer.

“This is the significant discovery”, she said.

Link to publication:

https://www.nature.com/articles/s41467-021-22101-7

The oncogene AAMDC links PI3K-AKT-mTOR signaling with metabolic reprograming in estrogen receptor-positive breast cancer | Nature Communications

Fig. 1: AAMDC overexpression and amplification are associated with a subgroup of ER + breast cancer with poor prognosis. Fig. 2: AAMDC knockdown in luminal breast cancer cells inhibits tumorigenic ...

www.nature.com

Media assets: For video and head-shots of the lead author and laboratory footage please click on the following link: https://www.dropbox.com/sh/psq3n0o4smvp8to/AADSy9HGZv1gvqtIMjXxn2Kja?dl=0

About the Harry Perkins Institute of Medical Research                                     

The Harry Perkins Institute of Medical Research is one Australia’s leading medical research institutes investigating diseases affecting the community. With over 250 researchers located on three hospital campuses in Perth, the Perkins is uniquely positioned to fast track the development of new discoveries and treatments. It’s wholly owned clinical trials facility, Linear Clinical Research, provides international and local pharmaceutical and biotechnology companies the facilities to trial latest drugs and treatments in healthy volunteers and patients. The Harry Perkins Institute of Medical Research is proudly West Australian, providing career opportunities to our best and brightest graduates and bringing to the State international scientists. As a registered charity, the Harry Perkins Institute relies on grants and donations to fund its medical research.

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  • Gene found for deadliest breast cancer - published in Nature Communications

    Perth researchers discover new cancer-causing gene and protein for highly aggressive hard-to-treat cancer in sub-group of hormone sensitive breast cancers. Eight years work by Harry Perkins Institute of Medical Research and The University of Western Australia’s scientist Associate Professor Pilar Blancafort, has resulted in the discovery of a cancer gene responsible for a particularly aggressive breast cancer that is typically resistant to treatment. This research published in Nature Communications today...

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    Associate Professor Pilar Blancafort

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